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Unglycosylated Mtaa expresses an Mtab-like determinant

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Abstract

Antigenic polymorphism of the class I-like maternally transmitted antigen (Mta) is controlled by a maternally transmitted factor (Mtf) thought to reside in mitochondria. However, the mechanisms by which Mtf generates antigenic polymorphism are not known. To address this issue, we investigated a possible role of post-translational oligosaccharide addition in the formation of Mta determinants. We examined the expression of Mta on cytotoxic T lymphocyte (CTL) target cells cultured in tunicamycin (TM), a known inhibitor of asparagine(N)-linked glycosylation. Of 18 Mtab-specific CTL lines, 8 lysed TM-treated Mtaa targets. Furthermore, a subclone of one of these eight lines, 17D5.G2, lysed TM-treated targets from all Mtaa strains tested, regardless of H-2K/D haplotype. On the other hand, this CTL clone did not lyse TM-treated target cells from the Mta null, but H-2 expressing strain B10. CAS2. Therefore expression of this Mtab-like determinant is concordant with the expression of Mtaa and seems unlikely to represent a cross-reactive H-2K/D epitope. Our data suggest that an Mtab-like determinant is expressed on unglycosylated Mtaa molecules. Thus, N-linked oligosaccharides probably prevent the expression of an Mtab-like determinant on the Mtaa molecule. We discuss how Mtf may contribute to Mta polymorphism through glycosylation.

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Abbreviations

CAB:

Con A blast

CML:

cell-mediated lympholysis

Con A:

concanavalin A

CTL:

cytotoxic T lymphocyte

DMEM:

Dulbecco's modified minimum essential medium

FCS:

fetal calf serum

IL-2:

interleukin-2

LPS:

lipopolysaccharide

mAb:

monoclonal antibody

MLC:

mixed leukocyte culture

mMDM:

modified Mishell-Dutton medium

Mta:

maternally transmitted antigen

NK:

natural killer

sMDM:

supplemented Mishell-Dutton medium

TM:

tunicamycin

β 2m:

beta-2 microglobulin

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Han, A.C., Rodgers, J.R. & Rich, R.R. Unglycosylated Mtaa expresses an Mtab-like determinant. Immunogenetics 25, 234–240 (1987). https://doi.org/10.1007/BF00404693

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  • DOI: https://doi.org/10.1007/BF00404693

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